Canonical Allele Identifier: CA342587728

Gene: RPS27

Linked Data

• MyVariant Identifiers: chr1:g.153963691A>T (hg19) ; chr1:g.153991215A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991215A>T , CM000663.2:g.153991215A>T	GRCh38
NC_000001.10:g.153963691A>T , CM000663.1:g.153963691A>T	GRCh37
NC_000001.9:g.152230315A>T	NCBI36
NG_053102.2:g.5461A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.295A>T
ENST00000643794.1:c.228A>T	ENSP00000495765.1:p.Glu76Asp
ENST00000651669.1:c.107A>T MANE Select	ENSP00000499044.1:p.Lys36Ile
ENST00000368567.4:c.107A>T	ENSP00000357555.4:p.Lys36Ile
ENST00000392558.4:c.107A>T	ENSP00000376341.4:p.Lys36Ile
ENST00000477151.1:n.262A>T
ENST00000493224.5:n.373A>T
NM_001030.4:c.107A>T	NP_001021.1:p.Lys36Ile
NM_001030.6:c.107A>T MANE Select	NP_001021.1:p.Lys36Ile
NM_001349946.1:c.11A>T	NP_001336875.1:p.Lys4Ile
NM_001349947.1:c.11A>T	NP_001336876.1:p.Lys4Ile
NM_001349946.2:c.11A>T	NP_001336875.1:p.Lys4Ile
NM_001349947.2:c.11A>T	NP_001336876.1:p.Lys4Ile